Actavis Laboratories, FL, Inc. recalls Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufact

Recalled April 22, 2015 · FDA recall D-0488-2015 · Actavis Laboratories, FL

Hazard

Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell · FDA Class III

Units

2,628 bottles

Sold at

Nationwide

Description

Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell

Product

Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90

Manufacturer(s)

Actavis Laboratories, FL, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →